Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Ministry of Education, Southwest Minzu University, Chengdu, China.
Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Sichuan Province, Chengdu, China.
Anim Sci J. 2021 Jan-Dec;92(1):e13514. doi: 10.1111/asj.13514.
Previous research reported that KLF3 plays different roles in the regulation of adipose deposition across species. However, the exact function of KLF3 in goat subcutaneous adipocyte remains unknown. Here, the goat KLF3 gene was firstly cloned and showed that the mRNA sequence of the goat KLF3 gene was 1,264 bp (GenBank accession number: KU041753.1) and its coding sequence was 1,037 bp, encoding 345 amino acids with three classic zinc finger domains of KLFs family at its C-terminus. The alignment of the amino acid sequence of KLF3 among various species demonstrated that goat had the highest homology to that of sheep, presenting 99.4% similarity, while the homology similarity to that of mice presented only 93.62% in contrast. Furthermore, KLF3 had highest mRNA level in fat tissue and lowest level in the heart in comparison. Additionally, the mRNA level of KLF3 gradually tended to increase during adipogenesis. Interestingly, overexpression of KLF3 increased lipid accumulation. In line with this, the gain-of-function of KLF3 dramatically elevated the mRNA levels of TG synthetic genes and adipogenic maker genes (p < .01) . Moreover, overexpression of KLF3 upregulated all the potential target genes, except for C/EBPα. These results suggested that KLF3 is a positive regulator for subcutaneous adipocyte differentiation in goats.
先前的研究报告表明,KLF3 在不同物种的脂肪沉积调控中发挥着不同的作用。然而,KLF3 在山羊皮下脂肪细胞中的确切功能仍不清楚。本研究首次克隆了山羊 KLF3 基因,并发现其 mRNA 序列长 1264bp(GenBank 登录号:KU041753.1),编码区长 1037bp,编码 345 个氨基酸,其 C 端具有三个经典的 KLF 家族锌指结构域。KLF3 氨基酸序列在不同物种间的比对表明,山羊与绵羊的同源性最高,相似度为 99.4%,而与小鼠的同源性相似度仅为 93.62%。此外,KLF3 在脂肪组织中的 mRNA 水平最高,而在心脏中的水平最低。此外,KLF3 的 mRNA 水平在脂肪生成过程中逐渐升高。有趣的是,KLF3 的过表达增加了脂肪堆积。与之相一致的是,KLF3 的功能获得显著提高了 TG 合成基因和脂肪生成标志物基因的 mRNA 水平(p<0.01)。此外,KLF3 的过表达上调了所有潜在的靶基因,除了 C/EBPα。这些结果表明,KLF3 是山羊皮下脂肪细胞分化的正向调控因子。